Landmark superimposition for taxonomic identification

The identification of organisms is a time-consuming task even for highly specialized researchers. Many ways to accelerate the identification process have been devised – from pictorial keys to automatic, machine identification – with different degrees of success. This paper explores landmark configurations as an aid to taxonomic identification. The basic hypothesis rests on the analogy between human fingerprints and organism landmark configuration. Translated into biological terms, it asks whether individual landmark configurations can be used as diagnostic characteristics for species identification. Water mites of the genus Torrenticola were used as test organisms. The results show that identification can be made simpler through the use of landmark configurations.  © 2004 The Linnean Society of London, Biological Journal of the Linnean Society , 2004, 81 , 267–274.     

Chamber growth in ammonites inferred from colour markings and naturally etched surfaces of Cretaceous vascoceratids from Nigeria

Cretaceous Vascoceras and Jurassic Lytoceras show colour markings and etched surfaces representing original organic membranes between the septa. The main difference between the formation of ammonite and Nautilus chambers involved the continuous secretion of a gelatinous cameral liquid to support the ammonite mantle when it moved forward. The gel containing cyclically secreted membranes. here named pseudosepta, resembled the intra-cameral structures of the cuttlebone in Sepia. Pseudoscpta are attached to the shell wall in pseudosutures (Pseudoloben) which are particularly visible in the saddles of the septal suture and tend to mimic them. Their shape suggests reconstruction of posterior mantle shape during translocation. Drag-bands (Schleppstreifen) are spiral markings formed by the overlapping pseudosepta along the axial traces of the foliole folds. The chamber of ammonites was formed by a locally muscular mantle in a tripartite cycle: (1) the mantle initially remained attached to the saddles of the completed septal suture while muscular tissue within the umbilical lobes was contracted and rapidly reattached to the side of the lateral saddles; (2) the whole mantle subsequently crept forward by secreting a gelatinous matrix which contained telescoped membranes, with an adhesive function on pseudolobc flanks; (3) the mantle almost ceased to move within the sites of future lobules, but expanded and crept on before forming the mural and 'gutter' ridges of the septum. □ Ammonites, chamber growth, vascoceratids, LYTOCERAS, Nigeria.     

Effects of Constant and Variable Nitrogen Supply on Sunflower (Helianthus annuus L.) Leaf Cell Number and Size

The effects of nitrogen (N) availability on cell number andcell size, and the contribution of these determinants to thefinal area of fully expanded leaves of sunflower (Helianthusannuus L.) were investigated in glasshouse experiments. Plantswere given a high (N =315 ppm) or low (N=21 ppm) N supply andwere transferred between N levels at different developmentalstages (5 to 60% of final size) of target leaves. The dynamicsof cell number in unemerged (< 0.01 m in length) leaves ofplants growing at high and low levels of N supply were alsofollowed. Maximum leaf area (LA_max) was strongly (up to two-fold)and significantly modified by N availability and the timingof transfer between N supplies, through effects on leaf expansionrate. Rate of cell production was significantly (P<0.05)reduced in unemerged target leaves under N stress, but therewas no evidence of a change in primordium size or in the durationof the leaf differentiation–emergence phase. In fullyexpanded leaves, number of cells per leaf (N_cell), leaf areaper cell (LA_cell) and cell area (A_cell) were significantly reducedby N stress. WhileLA_cell and A_cellresponded to changeover treatmentsirrespective of leaf size, significant (P<0.05) changes inN_cellonly occurred when the changeover occurred before the leafreached approx. 10% of LA_max. There were no differential effectsof N on numbers of epidermal vs. mesophyll cells. The resultsshow that the effects of N on leaf size are largely due to effectson cell production in the unemerged leaf and on both cell productionand expansion during the first phase of expansion of the emergedleaf. During the rest of the expansion period N mainly affectsthe expansion of existing cells. Cell area plasticity permitteda response to changes in N supply even at advanced stages ofleaf expansion. Increased cell expansion can compensate forlow N_cellif N stress is relieved early in the expansion of emergedleaves, but in later phases N_cellsets a limit to this response.Copyright 1999 Annals of Botany Company Helianthus annuus, leaf expansion, leaf cell number, leaf cell size, nitrogen, leaf growth, sunflower.     

Covariation of morphological characters in the Triassic ammonoid Czekanowskites rieberi

The Triassic ammonoid Czekanowskites rieberi displays a covariation of morphological charac ters, which is rather common in ammonoids. Its morphological spectrum ranges from laterally compressed, involute, weakly ribbed forms to depressed, semiinvolute, strongly ribbed forms. In order to study this covariation, fifteen axially cut specimens have been analyzed by means of image analysis, which allows us to obtain the ontogenetic record of radii, area and perimeter of the individual whorl cross-sections. A logarithmic model of growth has been applied. Our data indicate that, owing to the covariation, the radii from the origin to the venter and to the umbil ical seam of a given whorl section vary inversely in order to maintain the relative position of the center of gravity of the whorl cross-section both throughout the ontogeny of single specimens and within the population. This influences hydrostatic parameters, such as the position of the center of mass and the orientation and stability of the shell. Since the ontogenetic record of the angular length of the body chamber is not known, we have calculated those hydrostatic varia bles using two mutually exclusive assumptions: (1) the angular length of the body chamber was constant throughout ontogeny and (2) the volume of the body chamber grew monotonically with the revolution angle. Fluctuations of the three hydrostatic variables were always less important in the first assumption. In any case, the spectrum of, for example, theoretical orien tations is comparable to those observed in the species of present-day Nautilus. The range of adult body-chamber length observed in C. rieberi is much narrower than the theoretical adult body-chamber length calculated under the second assumption which indicates that a certain control over this parameter existed in the natural population, probably in order to maintain a narrow range in orientation and stability. The excess or deficit in soft-body weight was probably compensated by inverse variations in shell-wall weight. The main conclusion is that, despite the extreme morphological variability, hydrostatic and, possibly, hydrodynamic properties of the population remained within narrow limits.     

Regulation of spiral growth in planorbid gastropods

Extensive experimentation has been performed on the planorbid Planorbarius metidjensis in order to determine which mechanism allows the snail to coil its shell regularly. Individuals of this species, like all Planorbidae, are permanently active and secrete their shells while crawling on the substrate. Experiments consisted of attaching weights to either side of the shell (which is carried almost vertically) in an umbilical position; these weights cause the shell to fall towards the substrate on the loaded side. It can be demonstrated, qualitatively and quantitatively, that during further growth the shell tube deviated initially (i.e. within the first half whorl after loading) towards the loaded side. In a later stage, when the animal is able to re-balance the shell-load complex by muscular activity, the shell tube gradually deviates away from the loaded side. This behaviour is to be expected if, after loading, secretion of the shell continued with the aperture parallel to the substrate and forming a constant angle with the direction of growth. The main implication is that in normal conditions the living posture largely controls the correct coiling of the shell. Minor experiments made with another planorbid species, Gyraulus laevis , confirm these conclusions. The growth pattern of planorbids requires that the snail has constant information on the orientation of the shell with respect to the substrate. This is permitted by the particular physiological ecology of this group, members of which, unlike terrestrial gastropods, are permanently active.     

Herpetomonas roitmani (Fiorini et al., 1989) N. Comb.: A Trypanosomatid with a Bacterium-like Endosymbiont in the Cytoplasm

The trypanosomatid previously described as Crithidia roitmani is characterized here at the ultrastructural and biochemical levels. The data indicates that the parasite belongs to the Herpetomonas genus, and we therefore suggest the flagellate to be denominated as Herpetomonas roitmani n. comb. Cladistic analysis of isoenzyme data generated by eight different enzymes showed that the parasite presented a distinct banding pattern and could be grouped with some Herpetomonas spp., but not with Crithidia spp., used as reference strains. Accordingly, when the parasites were grown for longer periods in Roitman's defined medium, expontaneous differentiation from promastigotes to opisthomastigotes (typical of the Herpetomonas genus) occurred. Transmission electron microscopy revealed the presence of bacterium-like endosymbionts in the cytoplasm of all evolutive forms of the parasite. All morphological alterations characteristic of endosymbiont-bearing trypanosomatids could be observed.